Results 71 to 80 of about 1,226,810 (157)

Three siblings with complete androgen insensitivity syndrome [PDF]

, 2013
A 27-year old woman presented with primary amenorrhoea and infertility. On examination, she was found to have palpable inguinal gonads, normal female external genitalia, a blind-ending vagina with no cervix, almost complete absence of axillary and pubic ...
Kemp, T
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Complete Androgen Insensitivity Syndrome

, 2018
Objective To determine whether androgen receptors affect the fatty acid profiles of neutral and polar lipids in human meibomian gland secretions. Methods Meibomian gland secretion samples were obtained from both eyes of (1) women with complete ...
Dana, Reza, Sullivan, Benjamin, Evans, James E., Cermack, Jennifer M., Sullivan, David   +4 more
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Androgen Insensitivity Syndrome: A Case Report of Clinical Intricacies [PDF]

Testicular Feminisation Syndrome, commonly termed as Androgen Insensitivity Syndrome (AIS), is a very uncommon genetic disorder. Although AIS patients are genetically male (46, XY), they may have all or some of the physical characteristics of females ...
R. Sahasra Serisha, Ganesh Guru
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Androgen receptor gene mutations in 46, XY females

Journal of Research in Medical Sciences, 2006
The androgen insensitivity syndrome is a heterogeneous disorder with a wide spectrum of phenotypic abnormalities, ranging from complete female to ambiguous forms that more closely resemble males.
Mir Davood Omrani, Soraya Saleh Gargari
doaj  

"Mixed germ cell testicular tumor" in an adult female

Journal of Human Reproductive Sciences, 2012
The androgen insensitivity (testicular feminization) syndrome was described by Morris in phenotypic females with 46XY karyotype, presenting with primary amenorrhea, adequate breast development, and absent or scanty pubic or axillary hair.
Udasimath Shivakumarswamy, R Purushotham, H K Kumar Naik, K R Nagesha   +3 more
doaj   +1 more source

A Case of Complete Androgen Insensitivity Syndrome [PDF]

, 2009
Androgen insensitivity syndrome, gonadectomy, estrogen supplementation a 23-year-old single female visited our gynecological clinic because of primary amenorrhea. The patient's breast development was good.
内藤, 愼二, 林田, 靖, 一瀬, 俊介, 計屋, 紘信, 大庭, 康司郎   +4 more
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Abstracts

Molecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source

Androgen insensitivity syndrome

, 2008
BACKGROUND: Androgen insensitivity is caused by mutations in the androgen receptor gene, and is a common etiological factor to ambiguous genitalia in the newborn.
Svensson, Johan, Giwercman, Yvonne,, Lund University.   +2 more
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Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies

, 2010
The androgen insensitivity syndrome (AIS) is a disease connected with the inactivation of AR due to a mutation that inactivate male sexual differentiation, and causes a spectrum of phenotypic anomalies having as a common aspect the loss of reproductive ...
Novelli, G, A. Malvasi, PACELLA, Elena, F. Laterza, A. Tinelli, E. Mazzone, A. A. Epifania, Epifania, AA, Mazzone, E, NOVELLI, GIUSEPPE, Novelli, A, G. Novelli, A. Novelli, Dell'Edera, D, Pacella, E, Vitullo, E, Malvasi, A, Laterza, F, D. Dell'Edera, Tinelli, A, E. Vitullo   +20 more
core   +1 more source

Morris syndrome: description of a case characterized by partial androgen insensitivity.

, 2010
The Morris syndrome is a X-linked recessive condition due to a complete or partial insensitivity to androgens, resulting in a failure of normal masculinization of the external genitalia in chromosomally male individuals.
Di Vito C, Smelzo S, Forchia F, De Stefano G, Chiancone F, Creta M, IMBIMBO, CIRO   +6 more
core   +2 more sources